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Cited 17 time in webofscience Cited 18 time in scopus
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dc.contributor.authorChen, WL-
dc.contributor.authorChou, CK-
dc.contributor.authorLin, MG-
dc.contributor.authorChen, YF-
dc.contributor.authorJee, SH-
dc.contributor.authorTan, HY-
dc.contributor.authorTsai, TH-
dc.contributor.authorKim, KH-
dc.contributor.authorKim, D-
dc.contributor.authorSo, PTC-
dc.contributor.authorLin, SJ-
dc.contributor.authorDong, CY-
dc.date.accessioned2015-06-25T02:17:07Z-
dc.date.available2015-06-25T02:17:07Z-
dc.date.created2010-01-18-
dc.date.issued2009-09-
dc.identifier.issn1083-3668-
dc.identifier.other2015-OAK-0000019786en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/10669-
dc.description.abstractBoth reflected confocal and multiphoton microscopy can have clinical diagnostic applications. The successful combination of both modalities in tissue imaging enables unique image contrast to be achieved, especially if a single laser excitation wavelength is used. We apply this approach for skin and corneal imaging using the 780-nm output of a femtosecond, titanium- sapphire laser. We find that the near-IR, reflected confocal (RC) signal is useful in characterizing refractive index varying boundaries in bovine cornea and porcine skin, while the multiphoton autofluorescence (MAF) and second- harmonic generation (SHG) intensities can be used to image cytoplasm and connective tissues (collagen), respectively. In addition, quantitative analysis shows that we are able to detect MAF from greater imaging depths than with the near-IR RC signal. Furthermore, by performing RC imaging at 488, 543, and 633 nm, we find that a longer wavelength leads to better image contrast for deeper imaging of the bovine cornea and porcine skin tissue. Finally, by varying power of the 780-nm source, we find that comparable RC image quality was achieved in the 2.7 to 10.7-mW range. (C) 2009 Society of Photo-Optical Instrumentation Engineers. [DOI: 10.1117/1.3247157]-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherSPIE-SOC PHOTOPTICAL INSTRUMENTATION-
dc.relation.isPartOfJOURNAL OF BIOMEDICAL OPTICS-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleSingle-wavelength reflected confocal and multiphoton microscopy for tissue imaging-
dc.typeArticle-
dc.contributor.college융합생명공학부en_US
dc.identifier.doi10.1117/1.3247157-
dc.author.googleChen, WLen_US
dc.author.googleChou, CKen_US
dc.author.googleDong, CYen_US
dc.author.googleLin, SJen_US
dc.author.googleSo, PTCen_US
dc.author.googleKim, Den_US
dc.author.googleKim, KHen_US
dc.author.googleTsai, THen_US
dc.author.googleTan, HYen_US
dc.author.googleJee, SHen_US
dc.author.googleChen, YFen_US
dc.author.googleLin, MGen_US
dc.relation.volume14en_US
dc.relation.issue5en_US
dc.relation.startpage54026en_US
dc.relation.lastpage54026en_US
dc.contributor.id10183385en_US
dc.relation.journalJOURNAL OF BIOMEDICAL OPTICSen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF BIOMEDICAL OPTICS, v.14, no.5, pp.54026 - 54026-
dc.identifier.wosid000271746100033-
dc.date.tcdate2019-01-01-
dc.citation.endPage54026-
dc.citation.number5-
dc.citation.startPage54026-
dc.citation.titleJOURNAL OF BIOMEDICAL OPTICS-
dc.citation.volume14-
dc.contributor.affiliatedAuthorKim, KH-
dc.identifier.scopusid2-s2.0-74049128998-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc12-
dc.description.scptc13*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusEXCITATION FLUORESCENCE MICROSCOPY-
dc.subject.keywordPlusSCANNING LASER MICROSCOPY-
dc.subject.keywordPlusBASAL-CELL CARCINOMA-
dc.subject.keywordPlus2ND-HARMONIC GENERATION-
dc.subject.keywordPlusHUMAN SKIN-
dc.subject.keywordPlusEX-VIVO-
dc.subject.keywordPlusCORNEA-
dc.subject.keywordPlusEYE-
dc.subject.keywordAuthormultiphoton fluorescence-
dc.subject.keywordAuthorsecond-harmonic generation-
dc.subject.keywordAuthorreflected confocal imaging-
dc.subject.keywordAuthoroptical microscopy-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryOptics-
dc.relation.journalWebOfScienceCategoryRadiology, Nuclear Medicine & Medical Imaging-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaOptics-
dc.relation.journalResearchAreaRadiology, Nuclear Medicine & Medical Imaging-

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